Shi Huan, Yun Peng, Zhu Yun, Wang Lu, Li Pingbo, Lou Guangming, Xia Duo, Zhang Qinglu, Xiao Jinghua, Li Xianghua, He Yuqing, Gao Guanjun
National Key Laboratory of Crop Genetic Improvement, Hubei Hongshan Laboratory, Huazhong Agricultural University, Wuhan, 430070 China.
Rice Research Institute, Anhui Academy of Agricultural Sciences, Hefei, 230031 China.
Mol Breed. 2022 Oct 24;42(11):68. doi: 10.1007/s11032-022-01328-2. eCollection 2022 Nov.
Rice grain size is a key determinant of both grain yield and quality. In this study, we conducted QTL mapping on grain size using a recombinant inbred line (RIL) population derived from a cross between variety Beilu130 (BL130) and variety Jin23B (J23B). A total of twenty-two QTL related to grain length (GL), grain width (GW), grain length-to-width ratio (LWR), grain thickness (GT), and thousand grain weight (TGW) were detected under two environments, and 14 of them were repeatedly detected. Two minor QTL, and , were validated and further delimited to regions of 631 kb and 272 kb, respectively. Parental sequence comparison of genes expressed in inflorescence in corresponding candidate regions identified frameshifts in the exons of and , both of which encode protein phosphatase 2C-containing protein, and , which encodes a BIM2 protein. Scanning electron microscopy (SEM) analysis revealed that the increase of cell size rather than cell number caused the differences in grain size between NILs of and . Quantitative RT-PCR analysis showed that the expression levels of , , , , , and were significantly different in both NILs and NILs. Our results lay the foundation for the cloning of and , and provide genetic materials for the improvement of rice yield and quality.
The online version contains supplementary material available at 10.1007/s11032-022-01328-2.
米粒大小是产量和品质的关键决定因素。在本研究中,我们利用品种北陆130(BL130)和品种金23B(J23B)杂交衍生的重组自交系(RIL)群体对粒型进行了QTL定位。在两种环境下共检测到22个与粒长(GL)、粒宽(GW)、长宽比(LWR)、粒厚(GT)和千粒重(TGW)相关的QTL,其中14个被重复检测到。验证了两个微效QTL,分别将其进一步定位到631 kb和272 kb的区域。对相应候选区域中在花序中表达的基因进行亲本序列比较,发现 和 的外显子存在移码,二者均编码含蛋白磷酸酶2C的蛋白, 编码一个BIM2蛋白。扫描电子显微镜(SEM)分析表明, 近等基因系之间粒型差异是由细胞大小增加而非细胞数量增加导致的。定量RT-PCR分析表明, 在 近等基因系和 近等基因系中的表达水平均存在显著差异。我们的结果为 和 的克隆奠定了基础,并为水稻产量和品质的改良提供了遗传材料。
网络版包含可在10.1007/s11032-022-01328-2获取的补充材料。